[Histonet] Harris Hematoxylin troubleshooting
|From:||Delatour =?iso-8859-1?Q?Beno=EEt?= |
I recently tried to do a H&E stain on mice brain frozen sections using a
protocol I sucessfully used with paraffin sections. Staining is very bad
with frozen sections, showing awful uneven labeling (i have just posted a
PDF file on http://www.histonet.org/ with some horrible pics ; the filename=20
Here are some details:
-Brains were fixed in buffered formaldehyde 10%, then cryoprotected with
DMSO-glycerol overnight and cut on a sliding microtome (40µm free floatting
sections). Sections were then mounted on Superfrost+ glass slides,
dehydrated overnight at 40°C and then processed for H&E staining.
-These sections can be perfectly stained using thionin, cresyl violet,
Vector nuclear fast red etc... They can also be processed with success for=20
IHC, histochemistry etc...
-My protocol is very (too?) simple: rehydratation in tap water - staining
in Harris H. (filtered) for 2-4 min - tap water - acidic alcohol ...
-My H&E attemps made use of the Harris hemtoxylin from (c)Roth (see
-The problem does not come from dewaxing as... brains were not embedded in=20
-The problem does not seem to come from to short rehydratation as 20 min
under tap water before hematein does not change anything.
-I have mounted sections on glass slides using gelatin-PBS or distilled
water : does not make any change.
-I have increased "incubation" times in the Harris solution (from 2 to 15
min): always uneven stain.
All suggestions/comments are welcome. Thanks!
Dr. B. Delatour
Laboratoire de Neurobiologie de l'Apprentissage,
de la Mémoire & de la Communication,
NAMC, CNRS UMR 8620, Bât 446
91405 Orsay Cedex, FRANCE
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